About us
Ctrlquality which carries on a business in the fields of ISO 13485 System Certification, CE Marking (CE in Machinery, CE in Lifts, CE in Building Materials, CE in Medical Devices), Ready-Mixed Concrete Certification/G Marking and Training, values the satisfaction and trust of its customers above everything. You can have a look at Our Accreditations and Authorities section to be informed on our service domains.
Ctrlquality’s professional staff, each one of which is experienced in their subject areas with their professional experience, is qualified enough to respond to all kinds of needs concerning the related activities.
Ctrlquality has set it as its goal not only to just control and confirm but also to provide added value to the systems of the firms it provides services for seeing them as its business partners while carrying out its activities without making concessions from impartiality. Accordingly, our experts have been ed from among experts capable of making comments from an objective perspective by combining experience with knowledge, generating solutions with constructive approaches and guiding the companies it provides services for in the activation of their systems.
Having adopted providing customer-oriented services as a principle since its foundation, Ctrlquality invests in technology, trainings and its staff to keep customer satisfaction at its best in order to be able to accomplish its goal.
Mission
To be the most reliable
In line with the principles of impartiality, independence and confidentiality, to provide the most reliable national and international certification, testing, verification and training services that are sensitive to human health and the environment, providing added value to its customers.
Vision
Being a World Brand
Owing to our sector experience and expert employees, to be the world leader conformity assessment body in the national and international arena by making a difference with an innovative and sustainable quality approach, without compromising our principles of impartiality, independence and confidentiality.
It is our basic policy to inform the relevant parties, to increase satisfaction by meeting the expectations and needs of all relevant parties in line with legal conditions, and to continuously improve ourselves based on national and international standards, to provide timely reliable service to customers within the framework of legal legislation, with independent, impartial, confidential, educated, professional and technical personnel who constantly renew and develop themselves, and by closely following current developments in the scope of services.
During the performance of TS EN ISO 13485 Medical Devices Quality Management System certification activities within the scope of TS EN ISO/IEC 17021-1 standard, product certification activities within the scope of TS EN ISO/IEC 17065 standard, product certification activities within the scope of 93/42/EEC Medical Device Directive, 2017/745/EU Medical Device Regulation, 2006/42/EC Machinery Safety Directive, 2014/33/EU Lifts Directive and 305/2011/EU Construction Products Regulation, greenhouse gas emission report verification activities within the scope of TS EN ISO/IEC 17029 standard and test activities within the scope of TS EN ISO/IEC 17025 standard, it is our duty to continuously improve our management system by ensuring compliance with the requirements of all other relevant legislation, harmonized standards and guides in addition to the above and stated ones.
General Manager
(G.02/11-10.10.2022/02.01.2008)
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